Prevalence and progression of mitochondrial diseases: A study of 50 patients

Muscle and Nerve

Volumn 28, Issue 6, 2003, Pages 690-695

  Arpa, Javier ^a   Cruz Martínez, Antonio ^a   Campos, Yolanda ^b   Gutiérrez Molina, Manuel ^a   García Rio, Francisco ^a   Pérez Conde, Concepción ^a   Martín, Miguel A ^b   Rubio, Juan C ^b   Del Hoyo, Pilar ^b   Arpa Fernández, Ana ^c   Arenas, Joaquín ^b  

^a HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^b HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^c HOSPITAL SEVERO OCHOA   (Spain)

Author keywords

Electromyography; Genetics; Mitochondrial disease; Nerve conduction; Prevalence; Survival

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BIOCHEMISTRY; CAUSE OF DEATH; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; FEMALE; GENDER; HUMAN; MALE; MOLECULAR BIOLOGY; MYOPATHY; NEUROPATHY; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; SURVIVAL RATE; URBAN AREA;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; DISEASE PROGRESSION; DNA, MITOCHONDRIAL; ELECTROMYOGRAPHY; EPILEPSIES, MYOCLONIC; FEMALE; HUMANS; LACTIC ACID; MALE; MELAS SYNDROME; MIDDLE AGED; MITOCHONDRIAL DISEASES; MUSCLE, SKELETAL; NEURAL CONDUCTION; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL; PHENOTYPE; SPAIN; SURVIVAL ANALYSIS;

EID: 0345306346     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.10507     Document Type: Article

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